A5083541582- Intraocular Surgery and Lenses
- Retinal Diseases and Treatments
- Corneal surgery and disorders
- Ocular Diseases and Behçet’s Syndrome
- Retinal and Optic Conditions
- Retinal Imaging and Analysis
- Ocular Surface and Contact Lens
- Ophthalmology and Visual Impairment Studies
- Vestibular and auditory disorders
- Protein Tyrosine Phosphatases
- Pharmaceutical studies and practices
- Bone Tumor Diagnosis and Treatments
- Retinal and Macular Surgery
- Hearing, Cochlea, Tinnitus, Genetics
- Otitis Media and Relapsing Polychondritis
- Vasculitis and related conditions
- Telemedicine and Telehealth Implementation
- Thyroid and Parathyroid Surgery
- Corneal Surgery and Treatments
- Yersinia bacterium, plague, ectoparasites research
- Glaucoma and retinal disorders
- Artificial Intelligence in Healthcare
- Sarcoma Diagnosis and Treatment
- Mitochondrial Function and Pathology
- Sarcoidosis and Beryllium Toxicity Research
Hospital Universitario La Paz
2022-2023
Great Ormond Street Hospital
2020-2022
University College London
2020-2022
University of Oxford
2022
Oxford Health NHS Foundation Trust
2022
Whipps Cross University Hospital
2020
Barts Health NHS Trust
2020
Complejo Hospitalario de Navarra
2011-2015
Bellvitge University Hospital
2015
Instituto de Salud Carlos III
2015
Nystagmus, a condition characterized by involuntary eye movements, can be classified into two primary categories: infantile nystagmus (IN) and acquired nystagmus. IN typically manifests within the first 3‐6 months of life idiopathic or associated with various ocular conditions, including inherited retinal dystrophies (IRD), albinism, congenital cataracts. Acquired appears later in life. Diagnostic approaches for involve comprehensive examinations, optical coherence tomography (OCT),...
Purpose: The purpose of this study is to report the long-term efficacy and safety 0.19 mg fluocinolone acetonide intravitreal implant (ILUVIEN ® ) in pseudophakic eyes with diabetic macular oedema a multi-ethnic patient cohort. Methods: This single-centre retrospective analysis patients persistent oedema, despite previous anti-vascular endothelial growth factor and/or steroid treatment, treated ILUVIEN according national guidelines. Patients follow-up less than 24 months were excluded. Best...
Non-syndromic pediatric cataracts are defined as opacification of the crystalline lens that occurs during first years life without affecting other organs. Given this disease is one most frequent causes reversible blindness in childhood, main objective study was to propose new responsible gene candidates would allow a more targeted genetic approach and expand our knowledge about disease. We present whole exome sequencing (WES) 20 Spanish families with non-syndromic previous negative result on...
In Brief Purpose: To evaluate a telemedicine model to follow up patients with exudative age-related macular degeneration and compare the time spent using this conducting office examinations. Methods: Results of evaluations were compared determine whether previously treated intravitreal injections needed additional treatment. The examinations included visual acuity measurement, fundus examination, optical coherence tomography. evaluation retinography images, tomography data obtained in...
High myopia is the most severe and pathological form of myopia. It occurs when spherical refractive error exceeds -6.00 diopters (SDs) or axial length (AL) eye greater than 26 mm. This article focuses on early-onset high myopia, an increasingly common condition that affects children under 10 years age can lead to other serious ocular pathologies. Through genetic analysis 21 families with this study seeks contribute a better understanding role genetics in disease propose candidate genes....
Early-onset high myopia (EoHM) is a disease that causes spherical refraction error of ≥−6 diopters before 10 years age, with potential multiple ocular complications. In this article, we report clinical and genetic study 43 families EoHM recruited in our center. A complete ophthalmological evaluation was performed, sample peripheral blood obtained from proband family members. DNA analyzed using customized next-generation sequencing panel included 419 genes related to disorders suspected...
W e report the case of a young child who presented with bilateral acute anterior uveitis in context suspected paediatric inflammatory multisystem syndrome temporally associated COVID-19 (PIMS-TS).The study was conducted accordance principles Declaration Helsinki.Written consent obtained from father as patient is minor.PIMS-TS novel condition that has emerged during pandemic, first reported United Kingdom April 2020.Conjunctivitis most common ocular manifestation.A 9-year-old girl to local...
Escleritis posterior bilateralBilateral scleritis a. Zurutuza,
Keratoconus is a corneal dystrophy that one of the main causes transplantation and for which there currently no effective treatment all patients. The presentation this disease in pediatric age associated with rapid progression, worse prognosis and, 15–20% cases, need transplantation. It multifactorial genetic variability, makes its study difficult. Discovering new therapeutic targets necessary to improve quality life In manuscript, we present results whole-exome sequencing (WES) 24 families...